Product Recalls in Hawaii

Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,399 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,399 in last 12 months

Showing 2188121900 of 47,764 recalls

DrugMarch 26, 2019· Medi-Physics Inc. dba GE Healthcare

Recalled Item: Thallous Chloride TI 201 Injection Recalled by Medi-Physics Inc. dba GE...

The Issue: Chemical Contamination: Trace amounts of an impurity was detected in the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 26, 2019· Molnlycke Health Care, Inc

Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...

The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 25, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Pravastatin Sodium Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2019· Hamilton Medical AG

Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...

The Issue: New software version for affected ventilators reduces the probability of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· Auro Pharmacies Inc. DBA Central Drugs

Recalled Item: Biotin 10 mg/mL Injection Recalled by Auro Pharmacies Inc. DBA Central Drugs...

The Issue: Failed pH Specification: product does not meet pH label claim.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Fayosim (levonorgestrel and ethinyl estradiol) tablets USP Recalled by Lupin...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 22, 2019· Newport Ingredients

Recalled Item: Maika'i Sweet Honey Nut Snack Mix Recalled by Newport Ingredients Due to...

The Issue: Notified by manufacturer of nut mix of recall due to undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha with software version VA30-mobile C-arm x-ray Material # Recalled...

The Issue: Continuous operation of the Cios Alpha at high tube outputs may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMarch 21, 2019· Better Made Snack Foods Inc.

Recalled Item: Better Made Snack Foods Family Size $3.99 Original Potato Chips Recalled by...

The Issue: Undeclared milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund